NDC 36987-2377

Giant Wild Rye

Giant Wild Rye

Giant Wild Rye is a Intradermal; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Nelco Laboratories, Inc.. The primary component is Leymus Condensatus Pollen.

Product ID36987-2377_46893e16-0a95-41cc-816f-c05a3a464967
NDC36987-2377
Product TypeHuman Prescription Drug
Proprietary NameGiant Wild Rye
Generic NameGiant Wild Rye
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL; SUBCUTANEOUS
Marketing Start Date1972-08-29
Marketing CategoryBLA / BLA
Application NumberBLA102192
Labeler NameNelco Laboratories, Inc.
Substance NameLEYMUS CONDENSATUS POLLEN
Active Ingredient Strength40000 [PNU]/mL
Pharm ClassesNon-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 36987-2377-3

30 mL in 1 VIAL, MULTI-DOSE (36987-2377-3)
Marketing Start Date1972-08-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 36987-2377-1 [36987237701]

Giant Wild Rye INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102192
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1972-08-29
Inactivation Date2019-10-21

NDC 36987-2377-4 [36987237704]

Giant Wild Rye INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102192
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1972-08-29
Inactivation Date2019-10-21

NDC 36987-2377-3 [36987237703]

Giant Wild Rye INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102192
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1972-08-29
Inactivation Date2019-10-21

NDC 36987-2377-2 [36987237702]

Giant Wild Rye INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102192
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1972-08-29
Inactivation Date2019-10-21

Drug Details

Active Ingredients

IngredientStrength
LEYMUS CONDENSATUS POLLEN40000 [PNU]/mL

OpenFDA Data

SPL SET ID:97c8bed1-efbd-4af1-b242-85f80edeee5b
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 889664
  • 1014697
  • 889563
  • 1044507
  • 1044244
  • 900014
  • 897353
  • 1044528
  • 899546
  • 992850
  • 900163
  • 1044614
  • 899978
  • 889527
  • 899592
  • 1044254
  • Pharmacological Class

    • Non-Standardized Pollen Allergenic Extract [EPC]
    • Increased Histamine Release [PE]
    • Cell-mediated Immunity [PE]
    • Increased IgG Production [PE]
    • Pollen [CS]
    • Allergens [CS]

    NDC Crossover Matching brand name "Giant Wild Rye" or generic name "Giant Wild Rye"

    NDCBrand NameGeneric Name
    36987-2373Giant Wild RyeGiant Wild Rye
    36987-2374Giant Wild RyeGiant Wild Rye
    36987-2375Giant Wild RyeGiant Wild Rye
    36987-2376Giant Wild RyeGiant Wild Rye
    36987-2377Giant Wild RyeGiant Wild Rye
    36987-2378Giant Wild RyeGiant Wild Rye
    36987-2379Giant Wild RyeGiant Wild Rye
    36987-2380Giant Wild RyeGiant Wild Rye

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.